DOTRIACONTANE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C32H66
Molecular Weight	450.8664
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC

InChI

InChIKey=QHMGJGNTMQDRQA-UHFFFAOYSA-N

InChI=1S/C32H66/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-32H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C32H66
Molecular Weight	450.8664
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Cytochrome P450 family member CYP704B2 catalyzes the {omega}-hydroxylation of fatty acids and is required for anther cutin biosynthesis and pollen exine formation in rice.	2010-01	20086189
Structure and growth of vapor-deposited n-dotriacontane films studied by X-ray reflectivity.	2009-11-17	19583228
Crystalline-to-plastic phase transitions in molecularly thin n-dotriacontane films adsorbed on solid surfaces.	2009-09-21	19778140
Coherent multidimensional vibrational spectroscopy of representative N-alkanes.	2009-09-10	19725584
Structure and phase transitions of monolayers of intermediate-length n-alkanes on graphite studied by neutron diffraction and molecular dynamics simulation.	2009-08-28	19725621
Root suberin forms an extracellular barrier that affects water relations and mineral nutrition in Arabidopsis.	2009-05	19461889
[Studies on chemical constituents of Daphne genkwa].	2009-04	19645232
Silencing of StKCS6 in potato periderm leads to reduced chain lengths of suberin and wax compounds and increased peridermal transpiration.	2009	19112170
The Arabidopsis cytochrome P450 CYP86A1 encodes a fatty acid omega-hydroxylase involved in suberin monomer biosynthesis.	2008	18544608
Estrogen-like activity of volatile components from Vitex rotundifolia L.	2007-07	17890827
Characterization of waxes used in pictorial artworks according to their relative amount of fatty acids and hydrocarbons by gas chromatography.	2006-01-06	16246351
Identification of fatty acid esters and hydrocarbon derivatives from Cyrtocarpa procera Kunth by GC-MS.	2006-01	16286300
Atomic force microscopy measurements of topography and friction on dotriacontane films adsorbed on a SiO2 surface.	2005-10-15	16252965
Ultrathin polymer film formation by collision-induced cross-linking of adsorbed organic molecules with hyperthermal protons.	2004-10-06	15453767
Effect of the polyoxyethylene chain length of triton X surfactants on the adsolubilization of reconstituted wax model compounds.	2002-02	11999401
[Studies on chemical constituents of Gaultheria leucocarpa var. Yunnanensis (Franch.) T. Z. Hsu & R. C. Fang].	2001-12	12776334
Discovery of novel trimethylalkanes in the internal hydrocarbons of developing pupae of Heliothis virescens and Helicoverpa zea.	2001-04	11290446

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:45:22 GMT 2025` Edited by `admin` on `Mon Mar 31 19:45:22 GMT 2025`
Record UNII	7KSV90RN23
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-6361

Preferred Name

English

DOTRIACONTANE

Systematic Name

English

N-DOTRIACONTANE

Common Name

English

Code System Code Type Description

FDA UNII

7KSV90RN23